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EAGER: Elucidating the Mechanism of Pseudophosphatase MK-STYX as a Regulator of mRNA Stability in the Stress Response Pathway

EAGER: Elucidating the Mechanism of Pseudophosphatase MK-STYX as a Regulator of mRNA Stability in the Stress Response Pathway
EAGER:阐明伪磷酸酶 MK-STYX 作为应激反应途径中 mRNA 稳定性调节剂的机制
批准号:
1113167
负责人:
Shanta Hinton
金额:
$30.0万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-05-01 至 2014-04-30

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中文摘要
翻译
当细胞暴露在高温或太阳紫外线等压力下时,它们会迅速做出反应以确保生存。 最快速的反应之一是停止蛋白质的产生,这使得细胞能够适应压力。 细胞通过将信使RNA(为蛋白质合成提供蓝图)隔离到称为应激颗粒的特殊隔室来维持这种控制。 一种名为G3 BP-1的信使RNA结合蛋白被广泛认为是应激颗粒的重要组成部分。 研究人员最近报道,另一种名为MK-STYX的蛋白质与G3 BP-1相互作用,抑制应激颗粒的形成。 虽然在过去的八年里,人们对应激颗粒进行了广泛的研究,但大多数研究都集中在G3 BP-1和其他参与调节应激颗粒组装的组分上。 本研究探讨了MK-STYX在分解应力颗粒和阻止其形成方面的新作用。 这项研究将提供深入了解MK-STYX在应激反应中的作用,作为信使RNA稳定性的调节剂和应激颗粒形成的动力学。 将解决以下具体目标:(1)确定MK-STYX对负责蛋白质产生的细胞途径的影响。 MK-STYX是否间接激活或绕过这一途径来阻断应激颗粒的组装? MK-STYX是否稳定蛋白质的产生,从而防止应激颗粒的形成,或者它是它们分解所必需的? (2)确定MK-STYX对应激颗粒组装所需的G3 BP-1复合物的影响。 MK-STYX是否会破坏G3 BP-1和其他支架蛋白之间的相互作用,这些蛋白是应力颗粒组装所必需的? (3)确定MK-STYX对细胞骨架和应激颗粒动力学所需的分子伴侣的影响。 MK-STYX是否与分解所需的热休克蛋白(如Hsp 70)相互作用?更广泛的影响。 该项目提供了将研究和教育无缝结合的机会。 它将使调查员能够加强威廉玛丽学院的生物课程,并为代表性不足的学生树立积极的榜样。 研究者的目标之一是设计生物化学的讲座和实验室课程,这将使学生了解蛋白质-蛋白质相互作用及其功能的研究。 她的研究目标和结果将纳入她的教学。 研究者一直致力于提高科学中代表性不足的群体的参与计划。 然而,她已经意识到,仅仅是一名教师是不足以留住非裔美国人和其他少数民族的科学。 必须鼓励来自代表性不足群体的个人获得博士学位,成为独立的调查人员。 调查员还将参加HHMI资助的计划,为代表性不足的群体提供独特的本科研究经验,并促进与当地历史上黑人服务机构的合作,如汉普顿大学,诺福克州立大学和弗吉尼亚州立大学,以促进教师和学生之间的专业发展和指导关系。 研究员将继续为她的学生提供真实的研究机会,使他们能够参与科学发现的激动人心的过程。
英文摘要
When cells are exposed to stress such as high temperature or ultraviolet rays from the sun, they respond quickly to ensure survival. One of the most rapid responses is stopping protein production, which allows cells to adapt to stress. Cells maintain this control by sequestering messenger RNAs, which provide the blueprint for protein synthesis, to special compartments called stress granules. A messenger RNA binding protein named G3BP-1 is widely accepted as an important component of stress granules. Researchers recently reported that another protein called MK-STYX interacts with G3BP-1 and inhibits stress granule formation. Although stress granules have been studied extensively for the past eight years, most studies have focused exclusively on G3BP-1 and other components involved in regulating stress granule assembly. This research explores the novel role MK-STYX has in disassembly of stress granules and in blocking their formation. This study will provide insight into the role MK-STYX plays in the stress response, as a regulator of messenger RNA stability and in the dynamics of stress granule formation. The following specific aims will be addressed: (1) Determine the effect of MK-STYX on the cellular pathway responsible for protein production. Does MK-STYX indirectly activate or bypass this pathway to block stress granule assembly? Does MK-STYX stabilize protein production, which would prevent stress granule formation, or is it required for their disassembly? (2) Determine the effect of MK-STYX on the G3BP-1 complex required for stress granule assembly. Does MK-STYX disrupt interactions between G3BP-1 and other scaffold proteins, which are required for stress granule assembly? (3) Determine the effect of MK-STYX on the cell cytoskeleton and chaperones required for stress granule dynamics. Does MK-STYX interact with heat shock proteins required for disassembly, such as Hsp70?Broader Impacts. This project provides the opportunity to integrate seamlessly research and education. It will allow the investigator to enhance the biology curriculum at the College of William & Mary and to serve as a positive role model for underrepresented students. One of the investigator's goals is to design a lecture and laboratory course in biological chemistry, which will expose students to the study of protein-protein interactions and their function. Aims and results of her research will be incorporated into her teaching. The investigator has always been committed to programs that enhance participation of underrepresented groups in science. However, she has realized that just being a faculty member is not enough to retain African-Americans and other minorities in the sciences. It is imperative to encourage individuals from underrepresented groups to obtain PhDs become independent investigators themselves. The investigator will also participate in an HHMI-funded program that provides underrepresented groups with a unique undergraduate research experience and that and promotes collaborations with local historically black-serving institutions such as Hampton University, Norfolk State University, and Virginia State University to foster professional development and mentoring relationships between faculty and students. The investigator will continue to provide real research opportunities for her students so that they may engage in the exciting process of scientific discovery.
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MK-STYX as a regulator in stress granule clearance
  • 批准号:
    1909316
  • 项目类别:
    Standard Grant
  • 资助金额:
    $90.0万
  • 财政年份:
    2019
  • 负责人:
    Shanta Hinton
  • 依托单位:
RIG: MK-STYX and PTEN Role(s) in Stress Granule Assembly and/or Disassembly
  • 批准号:
    0919651
  • 项目类别:
    Standard Grant
  • 资助金额:
    $19.94万
  • 财政年份:
    2009
  • 负责人:
    Shanta Hinton
  • 依托单位:
海外基金